PALS db: Putative Alternative Splicing database.
Journal: 2002/January - Nucleic Acids Research
ISSN: 1362-4962
PUBMED: 11752289
Abstract:
PALS db is a collection of Putative Alternative Splicing information from 19 936 human UniGene clusters and 16 615 mouse UniGene clusters. Alternative splicing (AS) sites were predicted by using the longest messenger RNA (mRNA) sequence in each UniGene cluster as the reference sequence. This sequence was aligned with related sequences in UniGene and dbEST to reveal the AS. This information was presented with six features: (i) literature aliases were used to improve the result of a gene name search; (ii) the quality of a prediction can be easily judged from the color-coded similarity and the scaled length of an alignment; (iii) we have clustered those EST sequences that support the same AS site together to enhance the users' confidence on a prediction; (iv) the users can also set up the alignment criteria interactively to recover false negatives; (v) tissue distribution can be displayed by placing the mouse cursor over an alignment; (vi) gene features will be analyzed at foreign sites by submitting the selected mRNA or its encoded protein as a query. Using these features, the users cannot only discover putative AS sites in silico, but also make new observations by combining AS information with tissue distributions or with gene features. PALS db is available at http://palsdb.ym.edu.tw/.
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Nucleic Acids Res 30(1): 186-190

PALS db: Putative Alternative Splicing database

Bioinformatics Program, Institute of Biochemistry, Bioinformatics Center and Department of Life Sciences, National Yang-Ming University, No. 155, Sec. 2, Li-Noun Street, Taipei, Taiwan 11221, Republic of China
To whom correspondence should be addressed. Tel: +886 2 2826 7128; Fax: +886 2 2826 4843; Email: yang@ym.edu.tw
Received 2001 Sep 6; Revised 2001 Oct 31; Accepted 2001 Oct 31.

Abstract

PALS db is a collection of Putative Alternative Splicing information from 19 936 human UniGene clusters and 16 615 mouse UniGene clusters. Alternative splicing (AS) sites were predicted by using the longest messenger RNA (mRNA) sequence in each UniGene cluster as the reference sequence. This sequence was aligned with related sequences in UniGene and dbEST to reveal the AS. This information was presented with six features: (i) literature aliases were used to improve the result of a gene name search; (ii) the quality of a prediction can be easily judged from the color-coded similarity and the scaled length of an alignment; (iii) we have clustered those EST sequences that support the same AS site together to enhance the users’ confidence on a prediction; (iv) the users can also set up the alignment criteria interactively to recover false negatives; (v) tissue distribution can be displayed by placing the mouse cursor over an alignment; (vi) gene features will be analyzed at foreign sites by submitting the selected mRNA or its encoded protein as a query. Using these features, the users cannot only discover putative AS sites in silico, but also make new observations by combining AS information with tissue distributions or with gene features. PALS db is available at http://palsdb.ym.edu.tw/.

Abstract

ACKNOWLEDGEMENTS

Y.-H.H. and Y.-T.C. were supported by grants from National Science Council, Taiwan (NSC 89-2323-B-010-003 and NSC 89-2318-B-010-011-M51, respectively). S.-T.Y. was supported by a grant from Veterans General Hospital, Tsing-Hua University and Yang-Ming University (VTY90-P5-40). The computational resource was supported by Ministry of Education, ROC (Program for Promoting Academic Excellence of Universities, 89-B-FA22-2-4).

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REFERENCES

REFERENCES

References

  • 1. Smith C.W. and Valcarcel,J. (2000) Alternative pre-mRNA splicing: the logic of combinatorial control. Trends Biochem. Sci., 25, 381–388. [[PubMed]
  • 2. Grabowski P.J(1998) Splicing regulation in neurons: tinkering with cell-specific control. Cell, 92, 709–712. [[PubMed][Google Scholar]
  • 3. Lahrtz F., Horstkorte,R., Cremer,H., Schachner,M. and Montag,D. (1997) VASE-encoded peptide modifies NCAM- and L1-mediated neurite outgrowth. J. Neurosci. Res., 50, 62–68. [[PubMed]
  • 4. Jiang Z.-H. and Wu,J.Y. (1999) Alternative splicing and programmed cell death. Proc. Soc. Exp. Biol. Med., 220, 64–72. [[PubMed]
  • 5. Yamamoto T., Nanba,E., Ninomiya,H., Higaki,K., Taniguchi,M., Zhang,H., Akaboshi,S., Watanabe,Y., Takeshima,T., Inui,K. et al. (1999) NPC1 gene mutations in Japanese patients with Niemann-Pick disease type C. Hum. Genet., 105, 10–16. [[PubMed]
  • 6. Gessler M., Konig,A. and Bruns,G.A. (1992) The genomic organization and expression of the WT1 gene. Genomics, 12, 807–813. [[PubMed]
  • 7. Dralyuk I., Brudno,M., Gelfand,M.S., Zorn,M. and Dubchak,I. (2000) ASDB: database of alternatively spliced genes. Nucleic Acids Res., 28, 296–297.
  • 8. Burset M., Seledtsov,I.A. and Solovyev,V.V. (2001) SpliceDB: database of canonical and non-canonical mammalian splice sites. Nucleic Acids Res., 29, 255–259.
  • 9. Christoffels A., Gelder,A.V., Greyling,G., Miller,R., Hide,T. and Hide,W. (2001) STACK: Sequence Taq Alignment and Consensus Knowledgebase. Nucleic Acids Res., 29, 234–238.
  • 10. Ji H., Zhou,Q., Wen,F., Xia,H., Lu,X. and Li,Y. (2001) AsMamDB: an alternative splice database of mammals. Nucleic Acids Res., 29, 260–263.
  • 11. Kan Z., Rouchka,E.C., Gish,W.R. and States,D.J. (2001) Gene structure prediction and alternative splicing analysis using genomically aligned ESTs. Genome Res., 11, 889–900.
  • 12. Kent W.J. and Zahler,A.M. (2000) The Intronerator: exploring introns and alterantive splicing in Caenorhabditis elegans. Nucleic Acids Res., 28, 91–93.
  • 13. Modrek B., Resch,A., Grasso,C. and Lee,C. (2001) Genome-wide detection of alternative splicing in expressed sequences of human genes. Nucleic Acids Res., 29, 2850–2859.
  • 14. Croft L., Schandorff,S., Clark,F., Burrage,K., Arctander,P. and Mattick,J.S. (2000) ISIS, the intron information system, reveals the high frequency of alternative splicing in the human genome. Nature Genet., 24, 340–341. [[PubMed]
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